• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
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    • 专利摘要:
    The invention relates to a device for taking a measurement of a dimension of a body part of a patient, said device comprising: - an electronic tape measure (12) comprising a portable housing (16), a winder (18) ) housed in the housing, a ribbon (20) partially wound on the reel and a section, said "unrolled section" (38), extends outside the housing, and a measuring module (22) d a measurement (M) relative to said unrolled section; a coherence control module (60) of said measurement (M) by means of at least one coherence rule and at least one context data, and an alert module (62) capable of delivering a alert in case of detection of an inconsistency by said coherence check module.
    公开号:FR3052655A1
    申请号:FR1655647
    申请日:2016-06-17
    公开日:2017-12-22
    发明作者:Sophie Bassez；Amina Ouchene
    申请人:Laboratoires Innothera SAS；
    IPC主号:
    专利说明:

    Measuring device for a measurement
    TECHNICAL FIELD The invention relates to a device for measuring a dimension of a body part of a patient, in particular for measuring the perimeters of a leg of a patient for a prescription of a patient. elastic venous compression brace, or CVE, indicated in case of venous insufficiency of a lower limb of a patient.
    State of the art
    Elastic venous compression orthoses, formerly known as "compression stockings" or "compression stockings", are textile medical devices that produce a therapeutic effect by compressing the lower limbs as opposed to the lower stockings. maintenance "(or" low support "or" low anti-fatigue ") and" low mode ", which are not medical devices for therapeutic purposes.
    Elastic venous compression orthoses are designed to produce a therapeutic effect by compressing the lower limb over a greater or lesser extent, usually with a decreasing compression profile upwardly from the ankle.
    The morphology of the lower limbs being different from one patient to another, a model of orthosis is classically declined in several sizes in order to satisfy the market.
    To determine the size of an elastic venous compression orthosis for a patient, it is necessary to measure different dimensions of his leg, including perimeters at different altitudes. In particular, measurements can be taken at standardized altitudes.
    To measure a perimeter, a conventional tape measure can be used. The quality of the measurement however depends on the operator in charge of this measurement.
    Reading the ribbon graduation can also cause parallax errors.
    The quality of the measurements is particularly important when they are used to choose an orthosis adapted to a particular pathology. The effectiveness of a treatment is indeed directly dependent on the good adequacy of the orthosis to the morphology of the patient. FR 2 788 957 proposes an electronic measuring device. This device comprises in particular an encoder capable of evaluating, without intervention of the operator, the length of the unwound ribbon. This device reduces the risk of error.
    However, there is a permanent need to improve the quality of the measurements made.
    An object of the present invention is to meet this need. SUMMARY OF THE INVENTION The invention proposes a measuring device of one dimension, and in particular a perimetric dimension of a body part of a patient, said device comprising: an electronic tape measure comprising a housing portable, a retractor housed in the housing, a ribbon partially wound on the reel and a section, called "unrolled section", extends outside the housing, and a measuring module of a measurement, relative to said unrolled section; a coherence control module of said measurement by means of at least one coherence control and at least one context data, and an alert module capable of delivering an alert in the event of detection of an inconsistency by said consistency check module.
    As will be seen in more detail in the following description, a measuring device according to the invention not only allows an electronic measurement, but also to verify that this measurement is compatible with the context in which the device has been used. In particular, in one embodiment, the measuring device makes it possible to verify that the measurement is compatible with the treatment applied and / or with measurements made previously.
    A device according to the invention may also comprise one or more of the following preferred optional features: said measurement is a function of the length of the unrolled section and / or a tension of the unrolled section and / or a position of the box and / or a position the unrolled section, in particular a plate of the case; said at least one context datum comprises at least one datum specific to the taking of said measure, called "particular context datum"; said at least one contextual data item is: personal data relating to the patient, and / or therapeutic data relating to a treatment applied to the patient, and / or measurement data relating to the nature of the measurement, and / or historical data relating to a measurement taken previously, for the patient or another patient similar to the patient and / or having undergone treatment identical to that of the patient, and / or preferably relative to a measurement of the same nature. the coherence control evaluates the compatibility of the measurement with a range of lengths and / or altitudes and / or plates and / or voltages, and / or the compatibility of the instant of taking said measurement with a time interval, preferably determined according to the context data; the coherence control module is configured to evaluate the origin and / or the intensity of an inconsistency and / or to evaluate the deviation of the measurement with a reference value; the device comprises an interface allowing selection and / or input of at least one context data by an operator and / or selection and / or input of at least one coherence control by an operator; the coherence control module and / or the alert module are arranged in the housing; alternatively, the device comprises a base separate from the tape measure, preferably a computer, a tablet or a telephone, the coherence control module and / or the alert module being disposed in said base, the base and the meter. ribbon comprising respective communication means adapted for communication, preferably wireless, between said base and said tape measure; - The base and the tape measure are able to communicate said measurement and / or an alert generated by the alert module and / or context data and / or a coherence control; the base comprises an analysis module configured to determine an orthotic size, said determination being dependent on said measurement if the coherence control module has not detected any inconsistency relating to said measurement; - The tape measure comprises: a pawl, preferably manually deactivatable, allowing the rotation of the reel in the direction of unwinding of the ribbon and, as said pawl is activated or deactivated, prohibiting or allowing, respectively, the rotation the winder in the direction of winding the ribbon, a spring tending to rotate the winder in the winding direction, and a fastener disposed at the free end of the ribbon, adapted for attachment to a region of housing fastener; said fastener is magnetic; - The device comprises a concave bearing surface, the radius of curvature of which is at any point of said bearing surface, between 2.0 and 15 cm, preferably between 2.5 and 15 cm; the housing comprises a slot, from which emerges said unrolled section, the slot opening in the immediate vicinity of the bearing surface or in the bearing surface, the attachment region being arranged on the side opposite to the slot with respect to the bearing surface; the ribbon is made of a hypoallergenic material. The invention also relates to a method for measuring a dimension of a part of a body of a patient by means of a device according to the invention. Preferably, the method comprises the following steps: a) application of the housing to said part of the body; b) partial unwinding of the ribbon and, if said dimension is a perimetric dimension, fixing the free end of the ribbon on the attachment region of the housing; c) deactivating the pawl so as to press the tape on said part of the patient's body, under the effect of the spring; d) triggering a measurement; e) independently of steps a) to d), but before step f), inputting and / or selecting at least one particular context data; f) checking, by said coherence control module, the consistency of the measurement with said particular context data; g) alert, by said alert module, in case of inconsistency, preferably by specifying the origin and / or the intensity of the inconsistency; (h) resumption of at least steps a) to d) and f) and g) in the event of an alert.
    If the dimension is a perimetric dimension, in step a) a concave bearing surface of the housing is preferably applied to said body part, preferably transversely to the general direction of said part of the patient's body (the axis of a leg, for example). The invention finally relates to a method for determining a size of elastic venous compression orthosis, said method comprising the following successive steps: A) taking a set of measurements according to a measurement method according to the invention, the set of measurements preferably comprising at least one measurement of a calf perimeter and an ankle perimeter; B) choosing an orthosis size corresponding to said set of measurements, according to a therapeutic treatment to be applied.
    Preferably, said set of measurements comprises a measurement of the length of leg or crotch.
    More preferably, the base or the tape measure comprises an analysis module configured to determine said size as a function of said set of measurements. Definitions - "Altitude", or "level", corresponds to a level in the vertical direction when the orthosis is worn by a patient standing upright, as shown in Figure 7 of the French standard NF G 30- 102, part B, which represents a leg-style "Hohenstein type". "Ribbon" conventionally means a long and narrow band. In the present description, a "ribbon" also includes a wire. - A "patient" is not limited to humans but includes any animal.
    BRIEF DESCRIPTION OF THE FIGURES Other features and advantages of the invention will become apparent on reading the detailed description which follows and on examining the appended drawing in which FIG. 1 diagrammatically represents a device according to the invention.
    detailed description
    FIG. 1 schematically represents a measuring device 10 according to the invention comprising a portable electronic tape measure 12 and a base 14 remote from the tape measure.
    The tape measure 12 conventionally comprises a housing 16, a reel 18 housed in the housing, a ribbon 20 partially wound on the reel 18 and a measuring module 22.
    Ribbon 20 is intended to surround a portion of the body of a patient to measure a perimeter dimension. This body part may be in particular an upper limb or a lower limb, and in particular a lower limb. For better accuracy, the tape may in particular be applied in contact with the skin of the patient. Preferably, it is a hypoallergenic material.
    The ribbon 20 preferably has a width greater than 1 cm, preferably greater than 2 cm and / or less than 5 cm, less than 4 cm, less than 3 cm, and / or a thickness of less than 1 mm, preferably less than 1 mm. at 0.5 mm, preferably less than 0.3 mm, and / or a length greater than 1 m, preferably greater than 1.3 m and / or less than 2 m, preferably less than 1.7 m, a length of 1.5 m being well adapted. The width and / or the thickness of the ribbon are preferably constant.
    Conventionally, the winder 18 has the general shape of a drum movable in rotation about its axis X. A first end of the ribbon 20 is fixed on the cylindrical side surface of the winder. The second end, or "free end" 26, of the ribbon 20 is free and extends outside the housing. A spring 30 tends to rotate the winder in a first direction, called "winding direction". The opposite sense is called "direction of flow".
    In a position called "rest position", almost all of the ribbon 20 is wound on the reel, only the free end 26 of the ribbon 20 extending outside the housing. Conventionally, the free end 26 comprises a stop 32 which, in the rest position, bears on the edge of a slot 36 formed in the housing 16 and through which the ribbon 20 passes.
    The unwinding of the ribbon 20 is performed conventionally by pulling on its free end 26, against the moment exerted by the spring 30 on the reel 18. The section 38 of the ribbon 20 which extends outside the casing is called "unrolled stretch". Unlike a mechanical tape measure, the electronic tape measure 12 further comprises a measurement module 22 capable of electronically determining a measurement M.
    The measurement module 22 may for example comprise a rotation encoder of the winder 18 or an encoder, for example optical or magnetic, detecting and counting marks 40 of the ribbon 20 passing in front of it, as described in FR 2 788 957, to evaluate the length Lss of the unrolled section 38.
    Preferably, the marks 40 are graduations, for example in centimeters or inches. Advantageously, the operator can thus evaluate approximately the length of the unrolled section by simply reading the graduations, and, if necessary, verify that the electronic measurement provided by the tape measure is compatible with what he observes. The free end of the ribbon 20 preferably includes a fastener 42 adapted for temporary attachment to the housing. By "temporary" is meant that the fastener can be deactivated by simple manipulation. Preferably, the fastener only allows the free end of the ribbon to be fastened to a limited portion of the casing, called the "attachment region". The attachment region preferably has a surface area of less than 2 cm. preferably less than 1 cm 2.
    The nature of the fastener 42 is not limiting. The clip may for example take the form of a clip or a pin, the attachment region being configured accordingly. Preferably, the fastener is magnetic, the attachment region being made of a ferrous material.
    More preferably, the fastener 42 serves as a stop 32.
    Between the slot 36 and the attachment region 44, the housing 16 preferably defines a bearing surface 46, preferably substantially cylindrical. Preferably, the radius of curvature R46 of the bearing surface 46 is in all points between 2.0 and 15 cm, preferably between 2.5 and 15 cm. Preferably, the radius of curvature R46 is substantially constant, regardless of the point of the bearing surface 46 considered.
    Preferably, the bearing surface 46 extends angularly, preferably, over an angular sector a greater than 20 degrees, preferably greater than 30 degrees, preferably greater than 50 degrees, preferably greater than 60 degrees, and or less than 90 degrees, preferably less than 80 degrees, preferably less than 70 degrees.
    The width of the bearing surface 46, measured along the X axis, is preferably greater than 1 cm, and / or less than 5 cm, 4 cm, 3 cm or 2 cm. Preferably, the width of the bearing surface 46 is greater than the width of the strip, preferably greater than 1.05 times the width of the strip, and / or preferably less than two times, preferably less than 1.5. times, preferably less than 1.2 times the width of the ribbon. Preferably, the width of the bearing surface 46 is substantially constant.
    More preferably, the fastener 42 is shaped so that, in the attached position of the tape in which the fastener 42 is attached to the attachment region, the tape can extend the bearing surface 46, substantially without breaking. slope. Preferably, the slot 36 is formed on the bearing surface 46, preferably at one end of the bearing surface 46. Advantageously, the accuracy of the measurement is improved. The comfort for the patient is also increased.
    The median longitudinal plane of the bearing surface 46 and / or the median transverse plane of the reel 18 and / or the median longitudinal plane of the ribbon 20, perpendicular to the X axis, are preferably merged.
    Preferably, the tape measure 12 further comprises means for locking in position the partially unrolled tape, regardless of the degree of unwinding. In a preferred embodiment, these means comprise a pawl 50 allowing rotation of the winder in the direction of unwinding and, depending on whether the pawl is activated or deactivated, prohibiting or authorizing, respectively, the rotation of the winder 18 in the direction of winding. Preferably, the pawl 50 is activated by default. Preferably, it can be deactivated manually, preferably by pressing a deactivation button 52. The deactivation of the pawl 50 advantageously allows, after the free end 26 of the ribbon 20 has been attached, by the clip 42, to the region fastener 44, to come to press, under the effect of the spring 30, the tape 20 against the body of the patient. Advantageously, the accuracy of the measurement is improved.
    In one embodiment, the tape measure further comprises a voltage sensor 64 for measuring the voltage on the unrolled section 38.
    According to the invention, the measuring device 10 further comprises a coherence control module 60 and an alert module 62.
    The coherence check module 60 is intended to guarantee the quality of the measurement M determined by the measurement module 22. More specifically, the coherence check module 60 processes the measurement M in order to check its compatibility, according to one or more control units. R consistency, with one or more context data C.
    The measurement M can be in particular the length Lss of the unrolled section or a function of this length, for example the sum of the length Lss and the length L46 of the bearing surface 46.
    The measurement M can also be, for example, a measurement relating to the position of the tape measure 12, for example the attitude of the unrolled section. The attitude of the unrolled section is the angle between the general plane in which the unrolled section extends and a horizontal plane. The attitude can be evaluated for example with a level. For lower limb measurements, particularly in view of prescribing an elastic venous compression brace, the patient may be required to stand upright and straight during measurements.
    The measurement M can also be a measurement of the voltage T38 of the unrolled section 38 measured with the voltage sensor 64. The measurement M can also be an assembly comprising several of the measures mentioned above, for example the sum of the lengths L28 and L46. , and the tension Tss ·
    Preferably, the measurement M is time stamped.
    The context data may include general context data and context data.
    The general context data is data associated with the application in which the measurement device 10 is to be used, regardless of its particular use for the patient.
    Preferably, the context data comprises particular context data, specific to the use of the measuring device 10.
    For example, the measuring device may be provided for the measurement of perimeters of the leg at several reference altitudes for the prescription of an elastic venous compression orthosis. In such an application, regardless of the patient, a measurement M must belong to an acceptable range of measurements. This acceptable range of measures is an example of general context data.
    The particular context data may in particular comprise: - a personal data relating to the patient, for example a measurement, the age or the sex of the patient, - a therapeutic data of a treatment applied to the patient, for example a frequency provided for the measurements, according to their nature, or a planned evolution for measuring a perimeter, - measurement data relating to the nature of the measurement, in particular an altitude, for example along the leg, and / or relating to a trim of the housing and / or relating to a time at which the measurement must be made.
    The consistency rules make it possible to test the compatibility of the measurement M with the context data, and in particular the particular context data.
    A consistency rule may in particular verify the membership of the measure to a determined range based on at least one particular context data.
    A consistency rule preferably compares the length L38 or L38 + L46 with a range of acceptable lengths, preferably determined based on personal data and / or therapeutic data and / or measurement data, and, if the length n ' does not belong to this beach, considers it an inconsistency.
    A consistency rule makes it possible, for example, to check whether the attitude of the unrolled section 38 and / or the tension of the unrolled section 38 is compatible with the conditions provided for the nature of the measurement.
    A consistency rule can also check whether the measurement M is compatible with another previously performed measurement (historical measurement), preferably for the same patient or for a similar patient.
    A consistency rule can also verify whether the measurement M, or an evolution of the measured data is (are) compatible with the treatment applied to the patient (therapeutic data).
    Preferably, a consistency rule checks whether the instant of measurement M is compatible with a predetermined time interval for this measurement, for example as a function of the treatment applied to the patient and / or of one or more measurements carried out previously (historical data ).
    In a preferred embodiment, the coherence check module 60 is able to detect an inconsistency in the measurement, but also able to evaluate the origin of an inconsistency and / or to quantify the intensity of said inconsistency, for example calculating a difference between the measurement, or a function of the measurement, and a reference value, preferably determined according to context data, and particularly particular context data.
    The alert module 62 is intended to transmit to the operator and / or the database 14 information relating to the consistency check performed by the coherence check module 60.
    The alert module 62 may issue an alert A in case of inconsistency, but also, preferably, an information Annex I on the origin of the inconsistency and / or the intensity of the inconsistency. For example, the alert module 62 may indicate that the inconsistency detected is due to the incompatibility of the measurement M with a historical measurement or with the altitude at which the measurement of M has been performed. Preferably, the alert module 62 specifies, for example, the deviation of the measurement M with a reference value considered as normal.
    The coherence control module 60 and / or the alert module 62 may be arranged inside the housing 16.
    In one embodiment, the coherence control module and / or the alert module are arranged in the base 14. The base can be fixed, conventionally a computer, or mobile, for example a telephone or a tablet provided with an adapted application. The use of a "smartphone" type telephone is preferred.
    The tape-measure 12 and the base 14 comprise communication modules 72 and 74, respectively. The communication modules are preferably adapted for wireless transmission of information. The information exchanged between the tape-measure 12 and the base 14 may in particular comprise said measurement M and / or an alert A and / or an additional information I generated by the alert module and / or a context data item. and / or a coherence control system enabling the coherence module to evaluate said measurement. The integration of the control module and the warning module in the fixed base 14 advantageously reduces the size of the tape measure 12, and thus facilitate its handling during the measurement.
    Preferably, the measurement taking device 10 also comprises an interface 68, for example a keyboard and / or a button and / or a screen, for example tactile, allowing the operator to enter one or more context data. In particular, the interface 68 is preferably configured to allow a selection of the nature of the measurement, for example to specify whether it is a measurement of the ankle, calf or thigh, and / or a selection of data relating to the patient and / or his treatment.
    The location of the interface 68 is not limited. The interface 68 may be on the tape measure, on the base 14, or partially on the tape measure and partially on the base.
    Preferably, the measuring device 10 further comprises a trigger 70, for example in the form of a button, allowing the operator to set the time of the measurement. In particular, the operator can trigger the measurement only after having surrounded the patient's limb with the ribbon 20, fixed the fastener 42 to the attachment region 44, and then deactivated the pawl 50. In one embodiment, the measurement is triggered automatically, for example according to the voltage Tss or, for example, after attachment of the fastener 42 and deactivation of the pawl 50.
    In the absence of inconsistency, measure M is considered "validated". It is preferably displayed on the interface 68 and / or registered.
    In a preferred embodiment, the operator can record several validated M measurements to constitute a set of measures adapted to the selection of an orthosis size. The first and last measurements of such an assembly may for example be identified by a long press on the trigger 70, for example more than one second.
    In a preferred embodiment, the measuring device 10 further comprises an analysis module 76 configured to determine at least one orthotic size adapted to said set of measurements.
    The analysis module 76 therefore comprises means of communication with the coherence control module in order to receive the validated measurements M.
    Preferably, the analysis module 76 is in the tape measure or in the base, depending on whether the coherence control module is in the tape or in the base, respectively. Physical communication, for example wire or conductive tracks, is then possible.
    The analysis module 76 can be activated, for example, upon receipt of a last measurement, without intervention of the operator.
    The size determined by the analysis module 76 may for example be displayed on the interface 68. Of course, the analysis module 76 then comprises means of communication with the interface 68.
    The manufacture of a measuring device according to the invention does not pose any particular difficulty. In particular, the electronic modules, such as the coherence control module, the alert module, or the communication modules can be easily manufactured using conventional electronic tools, including a processor, a computer memory and software. The software conventionally comprises code instructions allowing, when these instructions are executed by the processor, to obtain the desired functions.
    The operation of the measuring device 10 is a direct result of the foregoing description.
    To carry out a measurement of a perimeter dimension, the operator can proceed as follows: In step a), he applies the bearing surface 46 to the corresponding part of the body, for example on one leg of the patient . He orients the tape measure according to the dimension to be measured. For example, to measure the perimeter of the calf, it orients the housing substantially transversely to the direction of the leg. In step b), it pulls on the free end 26 of the ribbon, which emerges from the slot 36 of the casing, so as to unroll a length of ribbon of sufficient length to bypass the leg and attach the clip 42 on the attachment region 44 of the housing.
    During this operation, the pawl 50 prevents any winding of the ribbon 20 on the reel under the effect of the spring 30. Generally, the length of the unrolled section 38, which projects out of the housing, is greater than the length strictly necessary for belting the leg. In step c), the operator acts on the deactivation button 52, which deactivates the pawl 50, and therefore allows a winding of the ribbon, under the effect of the spring 30, until the section unrolled or in close support on the surface of the leg. In step d), the operator triggers the measurement by pressing the trigger 70. In step e), independently of steps a) to d), but before step f), described above. after, a context data is recorded, for example entered by the operator.
    Preferably, at least one consistency rule tested by the consistency check module 60 uses a particular context data. In particular, it is advantageous to use historical data relating to the patient, and in particular historical measurements relating to measurements of the same nature, for example relative, such as measurement M, to a perimeter of calf, and / or relating to same patient. In this case, in particular, no context data needs to be entered by the operator. The operator can, for example, enter the altitude of the measurement, or an identification of the patient, for example by means of a touch screen (interface 68), preferably on the base 14. The location of the interface 68 n ' is not limited.
    Context data can be entered into the measuring device via the fixed base 14 and / or via the tape measure 12. Part of the context data can be entered via the meter. ribbon and part through the base. For example, it may be convenient to enter the altitude of the measurement using the tape measure 12, as described in FR 2 788 987, and to enter the identifier or personal data of the patient in the database.
    In a preferred embodiment, the coherence control module is integrated in the base. The communication module of the tape measure 12 then communicates the measurement made at the base. The coherence module can then process this measurement by means of a consistency check and possibly detect an inconsistency.
    In case of inconsistency, the coherence control module transmits information corresponding to the alert module 62 so that it warns the operator. In step f), the alert module sends the operator an alert A and / or an annex I information to indicate any inconsistency, preferably by specifying the origin and / or intensity of the inconsistency .
    Preferably, the warning module is integrated in the tape-measure 12. The operator can immediately redo a measurement taking into account the alert. The alert can be in particular sound or light. For example, the ribbon meter may beep and / or flash a red LED. In step h), the operator renews the measurement if an inconsistency has been detected.
    The measurement method is preferably used for the determination of a size of elastic venous compression orthosis. In step A), steps a) to h) described above are implemented repeatedly to acquire a set of measurements at altitudes, or "reference levels", appropriate for the choice of a size.
    Preferably, the set of measurements comprises at least one measurement of an ankle perimeter and a measurement of a perimeter of the calf, and preferably a measurement of a thigh perimeter and / or a hip perimeter.
    In a preferred embodiment, the device according to the invention is still used to measure a length of leg or crotch. In step B), the doctor or pharmacist may choose a size corresponding to said set of measurements, typically by means of a grid.
    In a preferred embodiment, the size is determined by the analysis module as a function of said set of measurements. Preferably, the analysis module is integrated in the tape measure or, preferably, in the base. Preferably, the analysis module proposes a size automatically, that is to say without particular intervention of the operator, otherwise, possibly, to launch an analysis software in said analysis module.
    As now clearly apparent, the invention provides means for improving the quality of perimeter dimension measurements, which leads to an improvement in the quality of the applied treatment.
    Of course, the invention is not limited to the embodiments described and shown, provided for illustrative and non-limiting purposes.
    In particular, a device according to the invention can also be used to measure different dimensions of a perimeter dimension, for example the length of a leg.
    权利要求:
    Claims (19)
    [1" id="c-fr-0001]
    A device for taking a measurement of a size of a body part of a patient, said device comprising: an electronic tape measure (12) having a portable housing (16), a retractor (18) housed in the housing, a ribbon (20) partially wound on the reel and a section, said "unrolled section" (38), extends outside the housing, and a measurement module (22) of a measurement ( M), relative to said unrolled section; a coherence control module (60) of said measurement (M) by means of at least one coherence rule and at least one context datum, and an alert module (62) capable of delivering an alert in case of detection of an inconsistency by said coherence check module.
    [2" id="c-fr-0002]
    2. Device according to the immediately preceding claim, wherein said measurement (M) is a function of the length of the unrolled section and / or a tension of the unrolled section, and / or a position of the housing and / or a position of the unrolled section.
    [3" id="c-fr-0003]
    3. Device according to any one of the preceding claims, wherein said at least one context data item comprises at least one data specific to the taking of said measure, called "particular context data", chosen from: a personal data relating to the patient and / or therapeutic data relating to a treatment applied to the patient, and / or measurement data relating to the nature of the measurement, and / or historical data relating to a measurement taken previously, for the patient or another patient similar and / or identical treatment, and / or relating to a similar measure.
    [4" id="c-fr-0004]
    Apparatus according to any one of the preceding claims, wherein the consistency rule verifies the membership of the measure (M) to a determined range based on at least one particular context data.
    [5" id="c-fr-0005]
    5. Device according to any one of the preceding claims, wherein the consistency rule evaluates the compatibility of the measurement (M) with a range of lengths and / or altitudes and / or plates and / or voltages, and / or the compatibility of the time of measurement with a time interval.
    [6" id="c-fr-0006]
    Apparatus according to any one of the preceding claims, wherein the coherence check module is configured to evaluate the origin and / or intensity of an inconsistency and / or to evaluate the deviation of the measurement (M ) with a reference value.
    [7" id="c-fr-0007]
    7. Device according to any one of the preceding claims, comprising an interface allowing selection and / or input of at least one context data by an operator and / or selection and / or input of at least one control room. consistency by an operator.
    [8" id="c-fr-0008]
    8. Device according to any one of the preceding claims, wherein the coherence control module and / or the alert module are arranged in the housing.
    [9" id="c-fr-0009]
    9. Device according to any one of claims 1 to 7, comprising a base separate from the tape measure, the coherence control module and / or the alert module being disposed in said base, the base and the tape measure. comprising respective communication means adapted for radio communication between said base and said tape measure.
    [10" id="c-fr-0010]
    10. Device according to the immediately preceding claim, wherein the base is a computer, a phone or a tablet.
    [11" id="c-fr-0011]
    11. Apparatus according to any one of the two immediately preceding claims, wherein the base comprises an analysis module configured to determine a size, said determination depending on said measurement if the coherence control module has not detected a inconsistency in the said measure.
    [12" id="c-fr-0012]
    12. Device according to any one of the preceding claims, wherein the tape measure comprises: a ratchet (50), manually deactivatable, allowing rotation of the reel in the direction of unwinding of the tape and, according to said ratchet is activated or deactivated, prohibiting or allowing, respectively, the rotation of the reel in the direction of a winding of the ribbon, a spring (30) tending to rotate the reel in the winding direction, and a fastener (42) disposed at the free end of the ribbon, adapted for attachment to a fastening region (44) of the housing.
    [13" id="c-fr-0013]
    13. Device according to the immediately preceding claim, wherein said fastener is magnetic.
    [14" id="c-fr-0014]
    14. Apparatus according to any one of the two immediately preceding claims, having a concave bearing surface (46), and wherein the housing comprises a slot (36) from which emerges said unrolled section, the slot opening in the immediate vicinity of the bearing surface or in the slot, the attachment region being disposed on the opposite side to the slot relative to the bearing surface.
    [15" id="c-fr-0015]
    15. A method of measuring a dimension of a portion of a body of a patient by means of a device according to any one of the preceding claims, claims 12 and 14 being applied, said method comprising the following steps: a) application of the housing to said body part; b) partial unwinding of the ribbon and, if said dimension is a perimetric dimension, fixing the free end of the ribbon on the attachment region of the housing; c) deactivation of the pawl, so as to stretch the ribbon under the effect of the spring; d) triggering a measurement; e) independently of steps a) to d), but before step f), inputting and / or selecting at least one particular context data; f) checking, by said coherence control module, the consistency of the measurement with said context data; g) alert, by said alert module, in case of inconsistency; h) recovery, at least steps a) to d) and f) and g) in the event of an alert;
    [16" id="c-fr-0016]
    16. Measuring method of a dimension according to the preceding claim, wherein the dimension is a perimeter dimension.
    [17" id="c-fr-0017]
    17. A method for determining a size of elastic venous compression orthosis, said method comprising the following successive steps: A) taking a set of measurements according to a measuring method according to any one of the two claims immediately. previous, the set of measurements comprising at least one measurement of a calf perimeter and an ankle perimeter; B) choosing an orthosis size corresponding to said set of measurements, according to a therapeutic treatment to be applied.
    [18" id="c-fr-0018]
    18. A method of determining a size of elastic venous compression orthosis according to the immediately preceding claim, wherein said set of measurements comprises a measurement of the length of leg or crotch.
    [19" id="c-fr-0019]
    A method of determining an elastic venous compression orthosis size according to any of the two immediately preceding claims, wherein the base or the tape measure comprises an analysis module configured to determine said size according to said set of measures.
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    同族专利:
    公开号 | 公开日
    RU2017121134A3|2020-09-29|
    FR3052655B1|2018-07-13|
    US10349867B2|2019-07-16|
    DE102017113117A1|2017-12-21|
    RU2017121134A|2018-12-17|
    RU2744149C2|2021-03-03|
    US20170360331A1|2017-12-21|
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    法律状态:
    2017-04-28| PLFP| Fee payment|Year of fee payment: 2 |
    2017-12-22| PLSC| Search report ready|Effective date: 20171222 |
    2018-05-29| PLFP| Fee payment|Year of fee payment: 3 |
    2020-04-27| PLFP| Fee payment|Year of fee payment: 5 |
    2021-04-28| PLFP| Fee payment|Year of fee payment: 6 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1655647A|FR3052655B1|2016-06-17|2016-06-17|DEVICE FOR MEASURING A MEASUREMENT|
    FR1655647|2016-06-17|FR1655647A| FR3052655B1|2016-06-17|2016-06-17|DEVICE FOR MEASURING A MEASUREMENT|
    DE102017113117.5A| DE102017113117A1|2016-06-17|2017-06-14|Device for determining a measured value|
    CA2970907A| CA2970907A1|2016-06-17|2017-06-15|Measuring device for a measurement|
    RU2017121134A| RU2744149C2|2016-06-17|2017-06-16|Device for taking measurements|
    US15/626,479| US10349867B2|2016-06-17|2017-06-19|Device for taking a measurement|
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